| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691163-109691329 | Common:3; Rare:38; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179933-110180184 | Common:2; Rare:71 | ||||
| chr6:110958676-110958781 | Common:1; Rare:45 | ||||
| chr6:110981959-110982100 | Common:2; Rare:68 | ||||
| chr6:111259164-111259387 | Common:2; Rare:77 | ||||
| chr6:112087409-112087691 | Rare:91 | ||||
| chr6:113971106-113971501 | Common:3; Rare:124 | ||||
| chr6:116100679-116100913 | Common:1; Rare:94 | ||||
| chr6:116254036-116254242 | Common:5; Rare:60 | ||||
| chr6:116279324-116279463 | Common:1; Rare:56 | ||||
| chr6:116279841-116280099 | Common:2; Rare:88 | ||||
| chr6:117602423-117602683 | Common:4; Rare:69 | ||||
| chr6:119349750-119349948 | Common:2; Rare:71 | ||||
| chr6:121334454-121334589 | Common:4; Rare:53 | ||||
| chr6:121334706-121334843 | Common:2; Rare:31 |